Research study to evaluate an investigational immunotherapy for advanced prostate cancer - BMS CA184043 |
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| Protocol Title | Cancer - Prostate - Research study to evaluate an investigational immunotherapy for advanced prostate cancer - BMS CA184043 |
| Summary | This research study is designed to determine if an investigational agent, known as ipilimumab, is safe and effective for advanced prostate cancer when it is given after radiotherapy. Ipilimumab is currently approved by the United States Food and Drug Administration (FDA) and other Health Authorities for the treatment of newly diagnosed or previously-treated unresectable metastatic melanoma. Ipilimumab is an immunotherapeutic agent that is intended to "turn on" your immune system which may allow your immune system to attack and kill cancer cells. About 800 patients throughout the world, approximately 300 in the United States, are expected to participate in this study. Participants may be in the study for 1 year or more, depending on how they respond to the study therapy. Participants in this trial may receive, at no cost, study-related: medical care, study medication, laboratory work and evaluations. Medical insurance is not necessary to participate in this study, and study-related travel/parking may be reimbursed. |
| Therapeutic Area | Cancer - Prostate |
| Age Range | Minimum Age : 18 |
| Purpose | This trial is designed to determine if advanced prostate cancer patients that are treated with radiotherapy plus the investigational drug ipilimumab live longer than those treated with radiotherapy and supportive care. |
| Who is Eligible? | To participate you must:
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Trial Locations per State
| Location | State | Address |
Trial Materials and Media
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